SA99191080B1 - تخليق مركبات ثنائي كبريتيد disulphidesومتعدد كبريتيد polysulphidesعضوية - Google Patents
تخليق مركبات ثنائي كبريتيد disulphidesومتعدد كبريتيد polysulphidesعضوية Download PDFInfo
- Publication number
- SA99191080B1 SA99191080B1 SA99191080A SA99191080A SA99191080B1 SA 99191080 B1 SA99191080 B1 SA 99191080B1 SA 99191080 A SA99191080 A SA 99191080A SA 99191080 A SA99191080 A SA 99191080A SA 99191080 B1 SA99191080 B1 SA 99191080B1
- Authority
- SA
- Saudi Arabia
- Prior art keywords
- sulfur
- polysulphide
- resin
- mercaptan
- reaction
- Prior art date
Links
- 229920001021 polysulfide Polymers 0.000 title claims abstract description 51
- 230000015572 biosynthetic process Effects 0.000 title description 6
- 238000003786 synthesis reaction Methods 0.000 title description 6
- 229920005989 resin Polymers 0.000 claims abstract description 76
- 239000011347 resin Substances 0.000 claims abstract description 76
- 238000000034 method Methods 0.000 claims abstract description 16
- 229920003053 polystyrene-divinylbenzene Polymers 0.000 claims abstract description 15
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 claims abstract description 11
- 239000003054 catalyst Substances 0.000 claims abstract description 8
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 48
- 229910052717 sulfur Inorganic materials 0.000 claims description 43
- 239000011593 sulfur Substances 0.000 claims description 43
- 238000006243 chemical reaction Methods 0.000 claims description 26
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 claims description 16
- 125000000524 functional group Chemical group 0.000 claims description 15
- 239000011148 porous material Substances 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 7
- 238000002360 preparation method Methods 0.000 claims description 7
- 125000003118 aryl group Chemical group 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 5
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 3
- 125000003916 ethylene diamine group Chemical group 0.000 claims description 3
- 239000004215 Carbon black (E152) Substances 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 239000005864 Sulphur Substances 0.000 claims description 2
- XAQHXGSHRMHVMU-UHFFFAOYSA-N [S].[S] Chemical compound [S].[S] XAQHXGSHRMHVMU-UHFFFAOYSA-N 0.000 claims description 2
- 229930195733 hydrocarbon Natural products 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 239000011541 reaction mixture Substances 0.000 claims description 2
- -1 polyethylene Polymers 0.000 abstract description 6
- 229920000768 polyamine Polymers 0.000 abstract description 5
- 239000004698 Polyethylene Substances 0.000 abstract description 4
- 229920000573 polyethylene Polymers 0.000 abstract description 4
- 125000004427 diamine group Chemical group 0.000 abstract 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 22
- 229910052757 nitrogen Inorganic materials 0.000 description 11
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 10
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 description 10
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 8
- YAJYJWXEWKRTPO-UHFFFAOYSA-N 2,3,3,4,4,5-hexamethylhexane-2-thiol Chemical compound CC(C)C(C)(C)C(C)(C)C(C)(C)S YAJYJWXEWKRTPO-UHFFFAOYSA-N 0.000 description 7
- 239000000376 reactant Substances 0.000 description 7
- 150000003512 tertiary amines Chemical group 0.000 description 7
- 239000011521 glass Substances 0.000 description 6
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 6
- WKAPDSOUKRNDLE-UHFFFAOYSA-N 2-prop-2-enoxyacetamide Chemical compound NC(=O)COCC=C WKAPDSOUKRNDLE-UHFFFAOYSA-N 0.000 description 5
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 4
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 4
- 239000000460 chlorine Substances 0.000 description 4
- 229910052801 chlorine Inorganic materials 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- KYVBNYUBXIEUFW-UHFFFAOYSA-N 1,1,3,3-tetramethylguanidine Chemical group CN(C)C(=N)N(C)C KYVBNYUBXIEUFW-UHFFFAOYSA-N 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 3
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 125000000753 cycloalkyl group Chemical group 0.000 description 3
- 239000012299 nitrogen atmosphere Substances 0.000 description 3
- 150000003141 primary amines Chemical class 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 230000009466 transformation Effects 0.000 description 3
- GUUVPOWQJOLRAS-UHFFFAOYSA-N Diphenyl disulfide Chemical compound C=1C=CC=CC=1SSC1=CC=CC=C1 GUUVPOWQJOLRAS-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000002808 molecular sieve Substances 0.000 description 2
- 239000000523 sample Substances 0.000 description 2
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 description 1
- 206010028980 Neoplasm Diseases 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- KSPMJHKUXSQDSZ-UHFFFAOYSA-N [N].[N] Chemical compound [N].[N] KSPMJHKUXSQDSZ-UHFFFAOYSA-N 0.000 description 1
- 238000005576 amination reaction Methods 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 230000003321 amplification Effects 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- HRQGCQVOJVTVLU-UHFFFAOYSA-N bis(chloromethyl) ether Chemical compound ClCOCCl HRQGCQVOJVTVLU-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 229920001429 chelating resin Polymers 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 description 1
- XGZRAKBCYZIBKP-UHFFFAOYSA-L disodium;dihydroxide Chemical compound [OH-].[OH-].[Na+].[Na+] XGZRAKBCYZIBKP-UHFFFAOYSA-L 0.000 description 1
- 150000002019 disulfides Chemical class 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N dodecane Chemical group CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- PJMICNUGBHGMKQ-UHFFFAOYSA-N ethane-1,1,2-triamine Chemical compound NCC(N)N PJMICNUGBHGMKQ-UHFFFAOYSA-N 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000003517 fume Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- AFFLGGQVNFXPEV-UHFFFAOYSA-N n-decene Natural products CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 238000003199 nucleic acid amplification method Methods 0.000 description 1
- 239000005077 polysulfide Substances 0.000 description 1
- 150000008117 polysulfides Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000002296 pyrolytic carbon Substances 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C319/00—Preparation of thiols, sulfides, hydropolysulfides or polysulfides
- C07C319/22—Preparation of thiols, sulfides, hydropolysulfides or polysulfides of hydropolysulfides or polysulfides
- C07C319/24—Preparation of thiols, sulfides, hydropolysulfides or polysulfides of hydropolysulfides or polysulfides by reactions involving the formation of sulfur-to-sulfur bonds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Lubricants (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9800660A FR2773799B1 (fr) | 1998-01-22 | 1998-01-22 | Synthese de disulfures et polysulfures organiques |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SA99191080B1 true SA99191080B1 (ar) | 2006-07-30 |
Family
ID=9522034
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SA99191080A SA99191080B1 (ar) | 1998-01-22 | 1999-02-17 | تخليق مركبات ثنائي كبريتيد disulphidesومتعدد كبريتيد polysulphidesعضوية |
Country Status (23)
| Country | Link |
|---|---|
| US (1) | US6020529A (https=) |
| EP (1) | EP0931789B1 (https=) |
| JP (1) | JP4426008B2 (https=) |
| KR (1) | KR100594332B1 (https=) |
| CN (1) | CN1163481C (https=) |
| AR (1) | AR014471A1 (https=) |
| AT (1) | ATE200898T1 (https=) |
| AU (1) | AU750805B2 (https=) |
| BR (1) | BR9900108A (https=) |
| CA (1) | CA2257487A1 (https=) |
| CZ (1) | CZ295773B6 (https=) |
| DE (1) | DE69900093T2 (https=) |
| ES (1) | ES2157680T3 (https=) |
| FR (1) | FR2773799B1 (https=) |
| GR (1) | GR3036193T3 (https=) |
| HU (1) | HU223079B1 (https=) |
| ID (1) | ID22956A (https=) |
| MY (1) | MY128349A (https=) |
| PL (1) | PL330969A1 (https=) |
| PT (1) | PT931789E (https=) |
| SA (1) | SA99191080B1 (https=) |
| SG (1) | SG74117A1 (https=) |
| ZA (1) | ZA99320B (https=) |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19854427A1 (de) * | 1998-11-25 | 2000-05-31 | Basf Ag | Verfahren zur Herstellung von organischen Disulfiden |
| DE19942395A1 (de) * | 1999-09-06 | 2001-03-08 | Bayer Ag | Verfahren zur Herstellung von Polythiopolycarbonsäuren |
| FR2808272B1 (fr) | 2000-04-28 | 2002-06-14 | Atofina | Procede de fabrication d'olefines sulfurees |
| JP5060036B2 (ja) * | 2005-09-29 | 2012-10-31 | Ｈｏｙａ株式会社 | ポリチオールオリゴマーの製造方法 |
| US8097229B2 (en) | 2006-01-17 | 2012-01-17 | Headwaters Technology Innovation, Llc | Methods for manufacturing functionalized inorganic oxides and polymers incorporating same |
| CN101475517B (zh) * | 2009-01-15 | 2012-08-15 | 河南大学 | 一种对称的含二硫键化合物的制备方法 |
| CN102010282B (zh) * | 2010-10-18 | 2014-04-16 | 四川大学 | 一种在水相中催化制备二芳基二硫化合物和二芳基二硒化合物的方法 |
| CN102391166A (zh) * | 2011-07-20 | 2012-03-28 | 彩虹集团公司 | 一种用于染料敏化太阳能电池的离子液体的制备方法 |
| EP3106488A1 (en) * | 2015-06-19 | 2016-12-21 | Université de Haute Alsace | Photobase-catalysed oxidative polymerisation of poly (disulphide)s |
| US10884182B2 (en) | 2017-06-02 | 2021-01-05 | Dsm Ip Assets B.V. | Thermally resistant radiation curable coatings for optical fiber |
| JP7364239B2 (ja) | 2017-11-03 | 2023-10-18 | コベストロ （ネザーランズ） ビー．ブイ． | 液体放射線硬化性ｓａｐ組成物でコーティングされたファイバーを含む水遮断システム |
| EP3802452A1 (en) | 2018-06-01 | 2021-04-14 | DSM IP Assets B.V. | Radiation curable compositions for coating optical fiber via alternative oligomers and the coatings produced therefrom |
| CN113165971A (zh) | 2018-12-03 | 2021-07-23 | Ms控股有限公司 | 用于涂布光纤的填充式可辐射固化组合物以及由其产生的涂层 |
| US11932571B2 (en) | 2019-05-24 | 2024-03-19 | Covestro (Netherland) B.V. | Radiation curable compositions for coating optical fiber with enhanced high-speed processability |
| JP7618588B2 (ja) | 2019-05-24 | 2025-01-21 | コベストロ （ネザーランズ） ビー．ヴィー． | 強化された高速加工性を備えた光ファイバーをコーティングするための放射線硬化性組成物 |
| EP4003927A1 (en) | 2019-07-31 | 2022-06-01 | Covestro (Netherlands) B.V. | Radiation curable compositions with multi-functional long-armed oligomers for coating optical fibers |
| CN111422942A (zh) * | 2020-03-23 | 2020-07-17 | 浙江工业大学 | 一种利用乙二胺基树脂同步还原-吸附水体中六价铬的方法 |
| CN115515784A (zh) | 2020-04-03 | 2022-12-23 | 科思创(荷兰)有限公司 | 多层光学器件 |
| KR20220164742A (ko) | 2020-04-03 | 2022-12-13 | 코베스트로 (네덜란드) 비.브이. | 자가-치유 올리고머 및 이의 용도 |
| CN115427853B (zh) | 2020-04-03 | 2026-03-13 | 科思创(荷兰)有限公司 | 自我修复光纤和用于制造其的组合物 |
| WO2022002909A1 (en) | 2020-06-30 | 2022-01-06 | Covestro (Netherlands) B.V. | Viscosity index improvers in optical fiber coatings |
| US11459345B2 (en) * | 2020-08-14 | 2022-10-04 | The Goodyear Tire & Rubber Company | Method for the synthesis of asymmetric polysulfides |
| CN116888221A (zh) | 2021-02-22 | 2023-10-13 | 科思创(荷兰)有限公司 | 提供低光泽涂层的方法 |
| CN113603656B (zh) * | 2021-10-08 | 2022-03-15 | 科迈化工股份有限公司 | 橡胶硫化促进剂mbts的生产工艺 |
| CN118176225A (zh) | 2021-10-29 | 2024-06-11 | 科思创(荷兰)有限公司 | 可自由基固化的组合物 |
| EP4511336A1 (en) | 2022-04-21 | 2025-02-26 | Covestro (Netherlands) B.V. | Radiation curable compositions for coating optical fibers |
| EP4532577A1 (en) | 2022-05-25 | 2025-04-09 | Covestro (Netherlands) B.V. | Process for providing low gloss coatings |
| WO2024042082A1 (en) | 2022-08-24 | 2024-02-29 | Covestro (Netherlands) B.V. | Process for providing low gloss coatings |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE648125A (https=) * | 1963-05-20 | |||
| US4623711A (en) * | 1985-08-21 | 1986-11-18 | Products Research & Chemical Corp. | Modified disulfide polymer composition and method for making same from mercaptan terminated disulfide polymer and diethyl formal mercaptan terminated polysulfide |
| DE68900007D1 (de) * | 1988-04-14 | 1990-10-04 | Elf Aquitaine | Verfahren zur herstellung von organischen di- und polysulfiden. |
| US5028259A (en) * | 1990-03-06 | 1991-07-02 | Henkel Research Corporation | Recovery of precious metal |
| FR2742144B1 (fr) * | 1995-12-11 | 1998-01-16 | Elf Aquitaine | Procede de preparation de disulfures et de polysulfures organiques en presence de resines polystyrene-divinylbenzene possedant des groupes amine primaire |
| FR2742145B1 (fr) * | 1995-12-11 | 1998-01-16 | Elf Aquitaine | Procede de preparation de disulfures et de polysulfures organiques en presence de resines polystyrene-divinylbenzene (ps-dvb) possedant des groupes guanidines ou amidines |
-
1998
- 1998-01-22 FR FR9800660A patent/FR2773799B1/fr not_active Expired - Fee Related
-
1999
- 1999-01-07 JP JP00183899A patent/JP4426008B2/ja not_active Expired - Fee Related
- 1999-01-12 PT PT99400062T patent/PT931789E/pt unknown
- 1999-01-12 EP EP99400062A patent/EP0931789B1/fr not_active Expired - Lifetime
- 1999-01-12 AT AT99400062T patent/ATE200898T1/de not_active IP Right Cessation
- 1999-01-12 ES ES99400062T patent/ES2157680T3/es not_active Expired - Lifetime
- 1999-01-12 DE DE69900093T patent/DE69900093T2/de not_active Expired - Lifetime
- 1999-01-15 KR KR19990000917A patent/KR100594332B1/ko not_active Expired - Fee Related
- 1999-01-15 MY MYPI99000171A patent/MY128349A/en unknown
- 1999-01-18 SG SG1999000107A patent/SG74117A1/en unknown
- 1999-01-18 ZA ZA9900320A patent/ZA99320B/xx unknown
- 1999-01-19 BR BR9900108-0A patent/BR9900108A/pt not_active Application Discontinuation
- 1999-01-19 CA CA002257487A patent/CA2257487A1/fr not_active Abandoned
- 1999-01-19 US US09/232,690 patent/US6020529A/en not_active Expired - Lifetime
- 1999-01-20 CZ CZ1999192A patent/CZ295773B6/cs not_active IP Right Cessation
- 1999-01-21 PL PL99330969A patent/PL330969A1/xx not_active IP Right Cessation
- 1999-01-21 HU HU9900155A patent/HU223079B1/hu not_active IP Right Cessation
- 1999-01-21 AU AU13178/99A patent/AU750805B2/en not_active Ceased
- 1999-01-22 ID IDP990044D patent/ID22956A/id unknown
- 1999-01-22 CN CNB991027612A patent/CN1163481C/zh not_active Expired - Lifetime
- 1999-01-22 AR ARP990100269A patent/AR014471A1/es active IP Right Grant
- 1999-02-17 SA SA99191080A patent/SA99191080B1/ar unknown
-
2001
- 2001-07-09 GR GR20010401041T patent/GR3036193T3/el not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| KR19990067908A (ko) | 1999-08-25 |
| ID22956A (id) | 1999-12-23 |
| HUP9900155A3 (en) | 2000-06-28 |
| DE69900093D1 (de) | 2001-06-07 |
| MY128349A (en) | 2007-01-31 |
| JPH11255738A (ja) | 1999-09-21 |
| AR014471A1 (es) | 2001-02-28 |
| KR100594332B1 (ko) | 2006-06-28 |
| HU9900155D0 (en) | 1999-04-28 |
| CZ295773B6 (cs) | 2005-11-16 |
| SG74117A1 (en) | 2000-07-18 |
| HUP9900155A2 (hu) | 1999-09-28 |
| ES2157680T3 (es) | 2001-08-16 |
| CN1232024A (zh) | 1999-10-20 |
| AU1317899A (en) | 2000-06-08 |
| FR2773799A1 (fr) | 1999-07-23 |
| CA2257487A1 (fr) | 1999-07-22 |
| PT931789E (pt) | 2001-09-28 |
| BR9900108A (pt) | 2000-07-25 |
| FR2773799B1 (fr) | 2000-02-18 |
| ZA99320B (en) | 1999-09-20 |
| JP4426008B2 (ja) | 2010-03-03 |
| HU223079B1 (hu) | 2004-03-29 |
| PL330969A1 (en) | 1999-08-02 |
| US6020529A (en) | 2000-02-01 |
| EP0931789B1 (fr) | 2001-05-02 |
| DE69900093T2 (de) | 2001-09-20 |
| CN1163481C (zh) | 2004-08-25 |
| AU750805B2 (en) | 2002-07-25 |
| GR3036193T3 (en) | 2001-10-31 |
| ATE200898T1 (de) | 2001-05-15 |
| EP0931789A1 (fr) | 1999-07-28 |
| CZ19299A3 (cs) | 1999-08-11 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| SA99191080B1 (ar) | تخليق مركبات ثنائي كبريتيد disulphidesومتعدد كبريتيد polysulphidesعضوية | |
| JP2014516926A (ja) | ポリスルフィドの調製方法 | |
| US9193680B2 (en) | Method for the preparation of poly(disulfide) polymers and gels | |
| DE69607648T2 (de) | Verfahren zur herstellung organischer disulfide und polysulfide in gegenwart von polystyrol-divinylbenzol (ps-dvb) resinen, die guanidin- oder amidin gruppen haben | |
| US20090012260A1 (en) | Process For Preparing Polysulfides, Polysulfides, And Their Use | |
| US5919971A (en) | Process for the synthesis of 3-mercaptopropionic acid esters | |
| JP3911025B2 (ja) | 有機ジスルフィドおよび有機ポリスルフィドの製造法 | |
| US5817716A (en) | Resins with a primary amine or guanidine function | |
| US2919262A (en) | Process for making polysulfide liquid polymers | |
| AU2018371973B2 (en) | Functionalised compounds | |
| CN117120517A (zh) | 制备硫共聚物的方法 | |
| JPH0569820B2 (https=) | ||
| CN120365562B (zh) | 聚硫化苯并噻唑类化合物及其制备方法 | |
| JP2008094916A (ja) | 新規なアンモニウム塩含有ポリマー、その製造方法およびそれを触媒に用いたエポキシ化合物の製造方法 | |
| CN109705346A (zh) | 不含氯化锂和添加剂的聚苯硫醚及其制备方法与应用 | |
| KR19990067456A (ko) | 유기 디설파이드 및 폴리설파이드의 제조 방법 | |
| MXPA98004635A (en) | Method for preparing polysulphures and organic disulfures in the presence of polystyrene-divinylbenzene (ps-dvb) resins which have guanidine or amid groups |